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1.
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
Clin Endocrinol (Oxf)
; 87(6): 725-732, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28734020
2.
Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center.
Pituitary
; 18(4): 561-7, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-25315032
3.
Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly.
Clin Endocrinol (Oxf)
; 78(4): 551-7, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-22967285
4.
Successful Pregnancies After Adequate Hormonal Replacement in Patients With Combined Pituitary Hormone Deficiencies.
J Endocr Soc
; 1(10): 1322-1330, 2017 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29264457
5.
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).
Eur J Endocrinol
; 175(2): K7-K15, 2016 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-27252485
6.
FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.
Endocr Connect
; 4(2): 100-7, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25759380
7.
Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort.
Growth Horm IGF Res
; 24(5): 180-6, 2014 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25116472
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